Canonical Allele Identifier: CA276414819
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864515

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173241T>G , CM000678.2:g.173241T>G GRCh38
NC_000016.9:g.223240T>G , CM000678.1:g.223240T>G GRCh37
NC_000016.8:g.163240T>G NCBI36
NG_000006.1:g.34104T>G
NG_059186.1:g.1591T>G
NG_059271.1:g.5395T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.212T>G MANE Select ENSP00000251595.6:p.Val71Gly
ENST00000251595.10:c.212T>G ENSP00000251595.6:p.Val71Gly
ENST00000397806.1:c.116T>G ENSP00000380908.1:p.Val39Gly
ENST00000482565.1:n.348T>G
ENST00000484216.1:n.181T>G
NM_000517.4:c.212T>G NP_000508.1:p.Val71Gly
NM_000517.6:c.212T>G MANE Select NP_000508.1:p.Val71Gly